Disease: High density lipoprotein measurement
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2296172
MACF1
1.000 0.080 1 39370145 missense variant A/G;T snv 0.19; 8.0E-06 4
rs629301
CELSR2
0.851 0.120 1 109275684 3 prime UTR variant G/T snv 0.74 22
rs823114
NUCKS1
1.000 0.040 1 205750404 upstream gene variant G/A snv 0.45 3
rs12328675
COBLL1
2 164684290 3 prime UTR variant T/C snv 0.13 4
rs1728918 0.827 0.160 2 27412596 upstream gene variant A/G;T snv 19
rs222826 0.851 0.120 2 146120964 regulatory region variant T/C snv 0.94 16
rs2943634 0.763 0.200 2 226203364 intergenic variant A/C;G snv 15
rs478442 0.851 0.120 2 21176344 intergenic variant G/C;T snv 18
rs562338 0.807 0.160 2 21065449 intergenic variant A/G snv 0.69 21
rs6759518
SLC30A3
0.851 0.120 2 27263727 intron variant G/C snv 5.5E-02 16
rs7607980
COBLL1
1.000 0.080 2 164694691 missense variant T/C snv 0.11 0.13 8
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs7621025
STAG1
3 136553404 intron variant T/A;C snv 3
rs7632505
SEMA5B
0.827 0.120 3 123019460 intron variant A/G snv 0.34 17
rs9816226
DGKG
1.000 0.080 3 186116710 intron variant A/T snv 0.82 5
rs11727676
HHIP
0.776 0.080 4 144737912 synonymous variant T/C snv 6.6E-02 6.4E-02 14
rs13107325
SLC39A8
0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 34
rs13114738
SLC39A8
0.851 0.120 4 102363708 intron variant C/A;T snv 16
rs1869717
MAML3
0.851 0.120 4 139829967 intron variant G/C snv 0.14 16
rs4691380
PDGFC
4 156798972 intron variant C/T snv 0.45 4
rs6533530 0.851 0.120 4 110810780 intergenic variant T/C snv 0.47 16
rs2307111
POC5
0.925 0.120 5 75707853 missense variant T/A;C snv 4.5E-06; 0.47 5
rs4704221
CERT1
0.851 0.120 5 75463358 intron variant T/A;C snv 16
rs5744680
POLK
0.851 0.120 5 75584065 intron variant G/A snv 0.55 18
rs7703051 0.851 0.120 5 75329662 intron variant C/A snv 0.38 18